Functional Imaging and Inhibitor Screening of Human Pancreatic Lipase by a Resorufin-Based Fluorescent Probe

Human pancreatic lipase (hPL) is a crucial digestive enzyme responsible for the digestion of dietary lipids in humans, and inhibition of hPL is effective in reducing triglyceride intake, thereby preventing and treating obesity. In this study, a series of fatty acids with different carbon chain lengths were constructed to the fluorophore resorufin based on the substrate preference of hPL. Among them, RLE was found to have the best combination of stability, specificity, sensitivity and reactivity towards hPL. Under physiological conditions, RLE can be rapidly hydrolyzed by hPL and released to resorufin, which triggered approximately 100-fold fluorescence enhancement at 590 nm. RLE was successfully applied for sensing and imaging of endogenous PL in living systems with low cytotoxicity and high imaging resolution. Moreover, a visual high-throughput screening platform was established using RLE, and the inhibitory effects of hundreds of drugs and natural products toward hPL were evaluated. Collectively, this study reports a novel and highly specific enzyme-activatable fluorogenic substrate for hPL that could serve as a powerful tool for monitoring hPL activity in complex biological systems and showcases the potential to explore physiological functions and rapid screening of inhibitors.


Introduction
Human pancreatic lipase (hPL) is secreted by the pancreas and released into the gastrointestinal system, where it collaborates with bile salts secreted by the liver to break down fats into fatty acids and glycerol [1,2]. hPL plays an important role in the regulation of lipid metabolism, as it catalyzes the hydrolysis of approximately 50% to 70% of dietary fat [3]. Therefore, the activity of hPL is essential for lipid absorption, and inhibition of hPL is effective in reducing triglyceride intake, thereby preventing and treating obesity [4]. Obesity and overweight are closely associated with diabetes, hypertension, hyperlipidemia, fatty liver, cardiovascular disease and many other metabolic diseases [5][6][7]. Treating obesity can significantly reduce the prevalence of chronic metabolic diseases and mortality [8].

Enzymatic Kinetics of hPL-Mediated RLE Hydrolysis
A kinetic study was carried out to estimate the kinetic parameters of RLE hydrolysis in hPL. RLE (previously dissolved in DMSO) was serially diluted to the desired concentrations (1, 2.5, 4.0, 7.5, 10.0, 12.0 and 15.0 µM) and mixed with hPL solution (1.5 µg/mL final concentration) in which the bile salt concentration was 0.1 mg/mL. The buffer was Tris-HCl. The change in the fluorescence spectrum was then measured at 590 nm. Data analysis was performed by nonlinear regression using GraphPad Prism 6 (GraphPad Software, San Diego, CA, USA).

Confocal Microscopic Imaging of PL in AR42J Cells
AR42J cells were cultured overnight in DMEM containing 10% fetal bovine serum (FBS) at 37 • C in 5% CO 2 , followed by coculture with 0.5 µM caerulein in FBS-free medium for 24 h [32]. After washing twice with medium, the cells were incubated with/without 25 µM orlistat (prepared in FBS-free medium) in a 5% CO 2 incubator for 30 min at 37 • C. RLE stock solution (20 mM) was diluted with FBS-free cell culture medium to a final concentration of 10 µM, and cells were then incubated with FBS-free cell culture medium containing RLE for a further 30 min at 37 • C. After washing three times with PBS, the cells were imaged under a confocal fluorescence microscope (Leica SP8, Wetzlar, Germany): blue channel, λ ex = 405 nm, λ em = 415-485 nm; red channel, λ ex = 552 nm, λ em = 580-600 nm.

Fluorescence Imaging of Monkey Pancreas Slices
Slices were prepared from a cynomolgus pancreas obtained from a 4-year-old male cynomolgus monkey from JOINN Lab (Suzhou, China). Monkey pancreas tissue was sliced to a thickness of 150 µm using a Microtome cryostat (Leica, Wetzlar, Germany) and placed in dish (Ø 20 mm). For the blank group, neither RLE nor inhibitors were added. For the experimental group, sections were incubated with PBS containing RLE (15 µM) for 30 min only. For the inhibitor group, sections were treated with orlistat (25 µM) for 15 min, then incubated with RLE (15 µM) for 30 min. Finally, the samples were examined with a confocal microscope (Leica SP8, Wetzlar, Germany); λ ex = 552 nm, λ em = 580-600 nm.

Molecular Docking Simulations
Docking simulations were performed using AutoDock Vina (1.2.3) to analyze the binding between RLE and hPL. hPL (PDB:1lpa) and RLE structures were preprocessed by AutoDockTools-1.5.7. Docking sites for RLE were defined as described in the literature [33]. The RLE was then docked to the active site, and the docking poses were scored by Vina 1.2.3. The apo-hPL or the hPL-RLE complex structure was solvated in a dodecahedron water box of TIP3 water molecules with a spacing of 1 nm in all directions from the walls of the box. The sodium chloride concentration was set to 0.15 M. The model systems were first energyminimized with the heavy atoms of protein and ligand using the steepest descent algorithm with a maximum 50,000 steps until the maximum force < 10.0 kJ/mol. The temperature was equilibrated to 310 K in the NVT ensemble for 1 ns (V-rescale thermostat), and then the model systems were equilibrated in the NPT ensemble at 1 bar for 1 ns (Parrinello-Rahman barostat) [34,35]. In the production phase, the temperature and pressure were kept at 310 K and 1 bar, respectively using a V-rescale thermostat and a Parrinello-Rahman barostat. All the model systems were implemented in 100 ns MD simulations. Trajectories of simulations were further analyzed and visualized by PyMOL (The PyMOL Molecular Graphics System 2.4.0a0 Open-Source, Schrödinger LLC., New York, NY, USA) and Discovery Studio Visualizer (BIOVIA Discovery Studio 2019, Dassault Systèmes, San Diego, CA, USA).

hPL Inhibition Assay
An RLE-based fluorescence assay was used to measure the residual activity of hPL in order to determine the inhibitory potential of various compounds on hPL, and orlistat was selected as a positive inhibitor. First, we evaluated the inhibitory effect of 94 natural products derived from herbs and 94 drugs on hPL. In our high-throughput screening system, 1 ug/mL hPL was used, and the final concentration of the 94 natural products derived from herbs and 94 drugs used was 10 µM. Other conditions were the same as in the selectivity experiments. Additionally, IC 50 values were determined for the compounds exhibiting the strong inhibitory activity for hPL.

Design, Synthesis and Sensing Mechanisms of RLE
Enzyme recognition moiety is an indispensable element for fluorogenic substrates that is extremely responsible for selective and sensitive interactions with the target enzyme of interest [36]. Herein, based on the substrate preference of hPL, a series of fatty acids with different carbon chain lengths was constructed to the fluorophore resorufin as the recognition moiety of hPL. Mechanistically, esterification of the hydroxyl group of resorufin reduces its electron donor ability and inhibits the intramolecular charge transfer (ICT) process. When the ester group was selectively recognized by the hPL and cleaved in the enzyme-catalyzed reaction, then fluorophore resorufin was released to yield fluorescence due to the recovery of ICT progress. The chemical structures of the six designed resorufin esters are depicted in Scheme 1. Experimental details of the synthesis and structural characterization of the six ester compounds are described in the Supplementary Information. The screening results show that the resorufin lauryl ester (RLE) had the best reactivity towards hPL ( Figure 1A), the molecular docking results show that RLE had a good affinity for hPL (−8.0 kcal/mol) and the distance between the carbonyl carbon of RLE and the hydroxyl oxygen of ser-152 of the hPL was extremely short (only 4.0 Å) ( Figure 1B). During the 100 ns molecular dynamics simulations, the RMSD distribution of RLE vibrated to a very limited extent, suggesting that RLE stably bound to the catalytic pocket of hPL ( Figure 1C). Furthermore, RMS fluctuation of the flap region (residues 237-261) was also dramatically steadied after combination with RLE ( Figure 1D), the removal and reorientation of which by the substrate resulted in the catalytic activation of hPL. The sensibility of the RLE towards hPL was then carefully investigated. RLE was stable in buffer (Tris-HCl, pH 7.4) at 37 • C. After co-incubation with hPL, RLE (Φ = 0.007) was rapidly hydrolyzed and released resorufin (Φ = 0.19, λ ex = 570 nm), with a significant increase in fluorescence at 590 nm ( Figure S1). High-performance liquid chromatography (HPLC) and high-resolution mass spectrometry (HRMS) demonstrated that the change in fluorescence correlated with the production of resorufin ( Figure S2). The mechanism of hPL sensing by RLE is described in Figure 2A.

Selectivity and Sensitivity of RLE towards hPL
Since substrate specificity is a vital property affecting the performance of acti based fluorogenic substrate analysis, we further scrutinized the specificity of the RLE hPL under physiological conditions [37]. As shown in Figure 2B, only hPL caused a nificant fluorescence enhancement at 590 nm, while there was no noticeable change other enzymes, including carboxylesterases (hCES1A and hCES2A), cholinester (AChE and BChE), carbonic anhydrase (CA), pepsin, trypsin and peptidase (FAP), as as human serum albumin (hSA), which means that RLE has a good selectivity tow hPL. RLE was rapidly hydrolyzed by hPL and released to resorufin, which triggered proximately 100-fold fluorescence enhancement at 590 nm ( Figure 2C). Furthermore photostability and chemical stability of RLE and its hydrolysis product, resorufin, w also examined ( Figures S3-S5). The fluorescence intensity of neither RLE nor resor changed markedly after 60 min of irradiation with a 550 nm xenon lamp, indicating RLE and resorufin have outstanding photostability. The fluorescence intensity of RL extremely weak over a wide pH range, whereas resorufin fluoresces strongly in the range of 6.5-10.5. These results indicate that RLE and resorufin have favorable chem stability. Various interfering factors, such as various amino acids (Cys, Ser, Lys, etc.) ganic ions (Fe 2+ , Cu + , CN − , etc.) and GSH, do not affect the fluorescence response of towards hPL. These observations indicate that RLE could serve as a highly desirable orogenic substrate for sensing hPL based on its unique enzymatic activity.

Scheme 1. Synthesis of resorufin ester derivatives.
Enzyme recognition moiety is an indispensable element for fluorogenic subst that is extremely responsible for selective and sensitive interactions with the targe zyme of interest [36]. Herein, based on the substrate preference of hPL, a series of acids with different carbon chain lengths was constructed to the fluorophore resoruf the recognition moiety of hPL. Mechanistically, esterification of the hydroxyl grou resorufin reduces its electron donor ability and inhibits the intramolecular charge tra (ICT) process. When the ester group was selectively recognized by the hPL and cle in the enzyme-catalyzed reaction, then fluorophore resorufin was released to yield rescence due to the recovery of ICT progress. The chemical structures of the six desi resorufin esters are depicted in Scheme 1. Experimental details of the synthesis and s tural characterization of the six ester compounds are described in the Supplementar formation. The screening results show that the resorufin lauryl ester (RLE) had the reactivity towards hPL ( Figure 1A), the molecular docking results show that RLE h good affinity for hPL (−8.0 kcal/mol) and the distance between the carbonyl carbon of and the hydroxyl oxygen of ser-152 of the hPL was extremely short (only 4.0 Å) (F 1B). During the 100 ns molecular dynamics simulations, the RMSD distribution of vibrated to a very limited extent, suggesting that RLE stably bound to the catalytic p of hPL ( Figure 1C). Furthermore, RMS fluctuation of the flap region (residues 237 was also dramatically steadied after combination with RLE ( Figure 1D), the remova reorientation of which by the substrate resulted in the catalytic activation of hPL. The sibility of the RLE towards hPL was then carefully investigated. RLE was stable in b (Tris-HCl, pH 7.4) at 37 °C. After co-incubation with hPL, RLE (Ф = 0.007) was ra hydrolyzed and released resorufin (Ф = 0.19, λex = 570 nm), with a significant increa fluorescence at 590 nm ( Figure S1). High-performance liquid chromatography (H and high-resolution mass spectrometry (HRMS) demonstrated that the change in flu cence correlated with the production of resorufin ( Figure S2). The mechanism of hPL ing by RLE is described in Figure 2A.

Selectivity and Sensitivity of RLE towards hPL
Since substrate specificity is a vital property affecting the performance of activity based fluorogenic substrate analysis, we further scrutinized the specificity of the RLE for hPL under physiological conditions [37]. As shown in Figure 2B, only hPL caused a sig nificant fluorescence enhancement at 590 nm, while there was no noticeable change with other enzymes, including carboxylesterases (hCES1A and hCES2A), cholinesterases (AChE and BChE), carbonic anhydrase (CA), pepsin, trypsin and peptidase (FAP), as wel as human serum albumin (hSA), which means that RLE has a good selectivity towards hPL. RLE was rapidly hydrolyzed by hPL and released to resorufin, which triggered ap proximately 100-fold fluorescence enhancement at 590 nm ( Figure 2C). Furthermore, the photostability and chemical stability of RLE and its hydrolysis product, resorufin, were also examined ( Figures S3-S5). The fluorescence intensity of neither RLE nor resorufin changed markedly after 60 min of irradiation with a 550 nm xenon lamp, indicating tha RLE and resorufin have outstanding photostability. The fluorescence intensity of RLE is extremely weak over a wide pH range, whereas resorufin fluoresces strongly in the pH range of 6.5-10.5. These results indicate that RLE and resorufin have favorable chemica stability. Various interfering factors, such as various amino acids (Cys, Ser, Lys, etc.), or ganic ions (Fe 2+ , Cu + , CN − , etc.) and GSH, do not affect the fluorescence response of RLE towards hPL. These observations indicate that RLE could serve as a highly desirable flu orogenic substrate for sensing hPL based on its unique enzymatic activity.

Selectivity and Sensitivity of RLE towards hPL
Since substrate specificity is a vital property affecting the performance of activity-based fluorogenic substrate analysis, we further scrutinized the specificity of the RLE for hPL under physiological conditions [37]. As shown in Figure 2B, only hPL caused a significant fluorescence enhancement at 590 nm, while there was no noticeable change with other enzymes, including carboxylesterases (hCES1A and hCES2A), cholinesterases (AChE and BChE), carbonic anhydrase (CA), pepsin, trypsin and peptidase (FAP), as well as human serum albumin (hSA), which means that RLE has a good selectivity towards hPL. RLE was rapidly hydrolyzed by hPL and released to resorufin, which triggered approximately 100-fold fluorescence enhancement at 590 nm ( Figure 2C). Furthermore, the photostability and chemical stability of RLE and its hydrolysis product, resorufin, were also examined ( Figures S3-S5). The fluorescence intensity of neither RLE nor resorufin changed markedly after 60 min of irradiation with a 550 nm xenon lamp, indicating that RLE and resorufin have outstanding photostability. The fluorescence intensity of RLE is extremely weak over a wide pH range, whereas resorufin fluoresces strongly in the pH range of 6.5-10.5. These results indicate that RLE and resorufin have favorable chemical stability. Various interfering factors, such as various amino acids (Cys, Ser, Lys, etc.), organic ions (Fe 2+ , Cu + , CN − , etc.) and GSH, do not affect the fluorescence response of RLE towards hPL. These observations indicate that RLE could serve as a highly desirable fluorogenic substrate for sensing hPL based on its unique enzymatic activity.

Enzymatic Kinetics of RLE Hydrolysis
Enzymatic kinetic behavior is another key property not only for quantitative applications of activity-based fluorogenic substrates but also for the further identification of enzyme inhibitors [38]. To this end, the linear range of the fluorescence response of RLE towards hPL was evaluated preliminary. As shown in Figure 3A,B, the fluorescence intensity increased with increasing enzyme concentration, with good linearity in the enzyme concentration range of 0.5-6.0 µg/mL. The detection limit of RLE for hPL was determined to be 0.369 µg/mL. The time fluorescence responses of RLE towards hPL also exhibited good linearity with an incubation time up to 10 min ( Figure S6). After that, the hydrolytic kinetics of RLE were carefully characterized using hPL as the enzyme source. As shown in Figure 3C,D, the hydrolytic behavior of RLE in hPL was consistent with classical Michaelis-Menten kinetics, and the corresponding Eadie-Hofstee plots provided evidence for this conclusion. RLE showed high affinity and good responsiveness to hPL (K m = 10.36 µM; V max = 0.86 nmol/min/µg/hPL). The great kinetic parameters and properties of the probe provided the basis for its further application to the detection of complex biological samples. mined to be 0.369 µg/mL. The time fluorescence responses of RLE towards hPL also exhibited good linearity with an incubation time up to 10 min ( Figure S6). After that, the hydrolytic kinetics of RLE were carefully characterized using hPL as the enzyme source. As shown in Figure 3C,D, the hydrolytic behavior of RLE in hPL was consistent with classical Michaelis-Menten kinetics, and the corresponding Eadie-Hofstee plots provided evidence for this conclusion. RLE showed high affinity and good responsiveness to hPL (Km = 10.36 µM; Vmax = 0.86 nmol/min/µg/hPL). The great kinetic parameters and properties of the probe provided the basis for its further application to the detection of complex biological samples.

Confocal Microscopic Imaging of PL in Living Cells and Tissue Slices
High specificity and excellent fluorescence properties enabled the probe to bio-image the activity of endogenous PL in living cells and tissues. Prior to performing cellular imaging, the cytotoxicity of RLE was evaluated by a cholecystokinin octapeptide (CCK-8) assay. As shown in Figure S7, cell viability remained above 80% after 48 h of incubation at high concentrations of RLE (50 µM), which means that the RLE has great biocompatibility. Subsequently, AR42J cells were treated with RLE (20 µM) at 37 °C for 30 min, and a marked fluorescent signal was observed in the red channel ( Figure 4C). On the contrary, the fluorescent signal was significantly reduced after the addition of a specific PL inhibitor, orlistat ( Figures 4G and S9). Furthermore, the specificity of RLE towards PL in AR42J cell preparations was investigated. The results indicate that RLE can be rapidly hydrolyzed and released resorufin in AR42J cells preparations, whereas hydrolysis of RLE can be significantly blocked by orlistat ( Figure S10). These results substantiate that RLE can be used for the sensing of endogenous PL in living cells.

Confocal Microscopic Imaging of PL in Living Cells and Tissue Slices
High specificity and excellent fluorescence properties enabled the probe to bio-image the activity of endogenous PL in living cells and tissues. Prior to performing cellular imaging, the cytotoxicity of RLE was evaluated by a cholecystokinin octapeptide (CCK-8) assay. As shown in Figure S7, cell viability remained above 80% after 48 h of incubation at high concentrations of RLE (50 µM), which means that the RLE has great biocompatibility. Subsequently, AR42J cells were treated with RLE (20 µM) at 37 • C for 30 min, and a marked fluorescent signal was observed in the red channel ( Figure 4C). On the contrary, the fluorescent signal was significantly reduced after the addition of a specific PL inhibitor, orlistat ( Figures 4G and S9). Furthermore, the specificity of RLE towards PL in AR42J cell preparations was investigated. The results indicate that RLE can be rapidly hydrolyzed and released resorufin in AR42J cells preparations, whereas hydrolysis of RLE can be significantly blocked by orlistat ( Figure S10). These results substantiate that RLE can be used for the sensing of endogenous PL in living cells.
Encouraged by the excellent detection capability of this probe, we further evaluated the ability of RLE to detect endogenous PL in monkey pancreatic tissues ( Figure 5). Similar to the cell imaging results, red-channel fluorescence was clearly captured in tissue sections after coincubation with RLE (15 µM) for 30 min (Figure 5D), while the fluorescent signal was significantly diminished following pretreatment of orlistat (Figures 5F and S11). In addition, the hydrolysis of RLE in monkey pancreatic tissue preparations was also significantly inhibited by orlistat ( Figure S12). These results demonstrate that RLE is a credible and useful molecular tool for in situ sensing and imaging of endogenous PL in living cells and tissue slices with good cell permeability, low cytotoxicity and high imaging resolution. after coincubation with RLE (15 µM) for 30 min (Figure 5D), while the fluorescent signal was significantly diminished following pretreatment of orlistat (Figures 5F and S11). In addition, the hydrolysis of RLE in monkey pancreatic tissue preparations was also significantly inhibited by orlistat ( Figure S12). These results demonstrate that RLE is a credible and useful molecular tool for in situ sensing and imaging of endogenous PL in living cells and tissue slices with good cell permeability, low cytotoxicity and high imaging resolution.

High-Throughput Screening of hPL Inhibitors Based on RLE
The superior anti-interference properties and sensitivity prompted us to establish a high-throughput screening method for hPL inhibitors to identify potential hPL inhibitors as antiobesity agents. In this case, a visual high-throughput assay was established to screen hPL inhibitors, using RLE as a fluorogenic substrate in a 96-well microplate. As shown in Figure S8, orlistat, a specific PL inhibitor, strongly inhibited hPL-catalyzed RLE after coincubation with RLE (15 µM) for 30 min (Figure 5D), while the fluorescent signal was significantly diminished following pretreatment of orlistat (Figures 5F and S11). In addition, the hydrolysis of RLE in monkey pancreatic tissue preparations was also significantly inhibited by orlistat ( Figure S12). These results demonstrate that RLE is a credible and useful molecular tool for in situ sensing and imaging of endogenous PL in living cells and tissue slices with good cell permeability, low cytotoxicity and high imaging resolution.

High-Throughput Screening of hPL Inhibitors Based on RLE
The superior anti-interference properties and sensitivity prompted us to establish a high-throughput screening method for hPL inhibitors to identify potential hPL inhibitors as antiobesity agents. In this case, a visual high-throughput assay was established to screen hPL inhibitors, using RLE as a fluorogenic substrate in a 96-well microplate. As shown in Figure S8, orlistat, a specific PL inhibitor, strongly inhibited hPL-catalyzed RLE

High-Throughput Screening of hPL Inhibitors Based on RLE
The superior anti-interference properties and sensitivity prompted us to establish a high-throughput screening method for hPL inhibitors to identify potential hPL inhibitors as antiobesity agents. In this case, a visual high-throughput assay was established to screen hPL inhibitors, using RLE as a fluorogenic substrate in a 96-well microplate. As shown in Figure S8, orlistat, a specific PL inhibitor, strongly inhibited hPL-catalyzed RLE hydrolysis in a dose-dependent manner, with an IC 50 value of 2.51 nM, which is consistent with its reported inhibitory activity (IC 50 = 6.16 nM) [39]. Subsequently, the inhibitory effect of 94 drugs commonly used in clinical practice and 94 natural products derived from Chinese medicine was determined ( Figure 6A,C). The heat map clearly shows that six strong inhibitors stood out with a remarkable hPL-inhibitory effect ( Figure 6A: 8h procyanidin, 9h carnosol, 10h sciadopitysin; Figure 6B: 8b ivermectin, 1d Raloxifene and 1F sorafenib tosylate). As shown in Figure 6B,D, the IC 50 values for procyanidin, carnosol and sciadopitysin were 0.55 µM, 0.58 µM and 1.36 µM, respectively; the IC 50 values for ivermectin, raloxifene and sorafenib tosylate were 1.75 µM, 5.63 µM and 15.56 µM, respectively. These results demonstrate that the RLE-based assay holds great promise for visual high-throughput screening of hPL inhibitors. strong inhibitors stood out with a remarkable hPL-inhibitory effect ( Figure 6A: 8h procyanidin, 9h carnosol, 10h sciadopitysin; Figure 6B: 8b ivermectin, 1d Raloxifene and 1F sorafenib tosylate). As shown in Figure 6B,D, the IC50 values for procyanidin, carnosol and sciadopitysin were 0.55 µM, 0.58 µM and 1.36 µM, respectively; the IC50 values for ivermectin, raloxifene and sorafenib tosylate were 1.75 µM, 5.63 µM and 15.56 µM, respectively. These results demonstrate that the RLE-based assay holds great promise for visual high-throughput screening of hPL inhibitors.

Conclusions
In summary, a novel and highly selective fluorescent probe (RLE) towards hPL was rationally designed based on the substrate preference of hPL. Under physiological conditions, RLE can be rapidly hydrolyzed by hPL and released to resorufin, which triggered approximately 100-fold fluorescence enhancement at 590 nm. The proposed RLE-based fluorescence assay offers a novel, practical and reliable tool for quantitative detection of PL activity in complex biospecimens and high-throughput screening of PL inhibitors, in addition to in situ sensing of endogenous PL activity in living cells and tissues, with high spatiotemporal resolution.
Supplementary Materials: The following supporting information can be downloaded at: www.mdpi.com/xxx/s1. Figure S1: The change in absorption spectrum of RLE (20 µM) in presence of hPL (10 µg/mL); Figure S2: (A) Representative LC-UV chromatograms of RLE incubation samples at 37 °C, UV detector was set at 440 nm; Figure S3: The effects of pH values on the fluorescence intensity of RLE and its metabolite Resorufin (5 µM), PMT Gain = 500 volts; Figure S4: The photostability of RLE (5 µM) and Resorufin (5 µM), following continuous illumination at 550 nm for different time, PMT Gain = 500 volts; Figure S5: Fluorescence responses of RLE (5 µM) to various analytes in aqueous solution. Relative fluorescence intensity (%) = Fluorescence intensity of adding analytes / Fluorescence intensity of hPL; Figure S6: The Linear in fluorescence intensity of RLE (5 µM) over time upon addition of hPL (1 µg/mL) in buffer at 37 °C: Figure S7: The cytotoxicity of RLE in

Conclusions
In summary, a novel and highly selective fluorescent probe (RLE) towards hPL was rationally designed based on the substrate preference of hPL. Under physiological conditions, RLE can be rapidly hydrolyzed by hPL and released to resorufin, which triggered approximately 100-fold fluorescence enhancement at 590 nm. The proposed RLE-based fluorescence assay offers a novel, practical and reliable tool for quantitative detection of PL activity in complex biospecimens and high-throughput screening of PL inhibitors, in addition to in situ sensing of endogenous PL activity in living cells and tissues, with high spatiotemporal resolution.